About Us

History 

2024

2024.10

- Renewal of Medical Device Manufacturing and Quality Management Standards Certificate (GMP) KTC-ABBA-21568
- Supervised by MFDS and Korea Testing Certification Institute (KTC)


2024.09

- Submission of Designated Audit Application to Financial Supervisory Service External Audit Report System


2024.08

- Lead Underwriting Agreement for KOSDAQ Listing with Hana Securities, Convertible Bond Issuance (Pre-IPO Investment)


2024.06

- RCPS Issuance: 1,748,810 Preferred Shares at KRW 6,290 per share, Totaling KRW 11,000,014,900 


2024.04

 - SME Certification 0010-2024-317952, Supervised by the Ministry of SMEs and Startups


2024.03

China Trademark Patent Registration for REVOSTEM (ไนๅšๆ€้ป›) No. 74344887

- Morocco Product Certification for Hilthera 4.0: 50624/2023/4381-2024/DM/DPS/DMP/18

2023~2020

2023.12

- $3 Million Export Tower Award – Korea International Trade Association

- Gyeonggi Province Export Achievement Award – Certificate No. 15121, supervised by the Ministry of SMEs and Startups

- Domestic ReWave Trademark Patent Registration – No. 40-2121470-0000


2023.11

- Official Distributor Status Granted to Shanghai REV-MED Co., Ltd. (Legal Entity Status Acquired in China)

- Inno-Biz Certification (Technology-Innovative Small Business) – Certificate No. R170605-01132, supervised by the Ministry of SMEs and Startups

- Tricell PRP Morocco Product Certification – Certification No. 50624/2023/4381-2024/DM/DPS/DMP/18

- Main-Biz Certification (Management-Innovative Small Business) – Certificate No. 230601-03281, supervised by the Ministry of SMEs and Startups



2023.08
- Establishment of Shanghai REV-MED Co., Ltd.

2022.10

- Issuance of Convertible Bonds (Pre-IPO Investment Secured)

- Veterinary Medical Device Manufacturing License Acquired

- Korea MFDS Approval (Class III): TriCell PRP UNI


2021.07

- Korea MFDS Approval (Class III): Blood Processing Device (NovaStem BC)

- Korea MFDS Approval (Class III): Bone Marrow Processing Device (NovaStem BMAC)


2020.11

- Inno-Biz Certification (Technology-Innovative Small Business)

- Korea MFDS Approval (Class III): Fat Separation Device (DUOCELL SVF KIT)


2020.04

- ISO 13485: 2018 Certification Acquired

- Hilthera 4.0 CE Certification Acquired

History


2024~

  • 2024.10



  • 2024.09


  • 2024.08


  • 2024.06

  • 2024.04

  • 2024.03 

Renewal of Medical Device Manufacturing and Quality Management Standards Certificate (GMP) KTC-ABBA-21568
Supervised by MFDS and Korea Testing Certification Institute (KTC)


Submission of Designated Audit Application to Financial Supervisory Service External Audit Report System

Lead Underwriting Agreement for KOSDAQ Listing with Hana Securities, Convertible Bond Issuance (Pre-IPO Investment)

RCPS Issuance: 1,748,810 Preferred Shares at KRW 6,290 per share, Totaling KRW 11,000,014,900


SME Certification 0010-2024-317952, Supervised by the Ministry of SMEs and Startups

China Trademark Patent Registration for REVOSTEM (ไนๅšๆ€้ป›) No. 74344887

Morocco Product Certification for Hilthera 4.0: 50624/2023/4381-2024/DM/DPS/DMP/18

2019~2017

2019.01

- Taiwan Medical Device Certification: Hilthera 4.0


2018.12

- Development and Commercialization of Bone Marrow Processing Device


2018.11

- World-Class Product Certification


2018.09

- Development of Large-Capacity 50ml Autologous Bone Marrow Processing Device


2018.03

- Opening of REV-MED Stem Cell Research Institute


2017.05

- Opening of Laser Division


2017.03

- Japan PMDA Approval: Blood Processing Device (Class III, TriCell PRP)  

2016~2009

2016.08

- Health Technology (NET) Certification 


2016.06

- China CFDA (NMPA) Approval: Blood Processing Device (Class III, TriCell PRP) 


2016.03

- Korean MFDS Approval: Bone Marrow Processing Device (Class III, TriCell BMC) 


2015.12

- Establishment of REV-MED International GmbH in Germany (Joint Venture) 


2015.01~2015.12

- Blood Processing Device Development (Gyeonggi Science and Technology Promotion Agency)


2014.07~2015.07

- Development of Autologous Bone Marrow-Derived Stem Cell and Nucleated Cell Concentration Kit 


2013.10

- Opening of Corporate Research Institute 


2012.10

- ISO 13485: 2012 Certification Acquired

- TriCell PRP CE Certification Acquired


2012.07

- Korean MFDS Approval: Blood Processing Device (Class III, TriCell PRP) 


2009.01

- Establishment of REV-MED Corporation

2023~2020

  • 2023.12




  • 2023.11








  • 2023.08

  • 2022.10



  • 2021.07


  • 2020.11


  • 2020.04 

$3 Million Export Tower Award – Korea International Trade Association

Gyeonggi Province Export Achievement Award – Certificate No. 15121, supervised by the Ministry of SMEs and Startups

Domestic ReWave Trademark Patent Registration – No. 40-2121470-0000


Official Distributor Status Granted to Shanghai REV-MED Co., Ltd. (Legal Entity Status Acquired in China)

Inno-Biz Certification (Technology-Innovative Small Business) – Certificate No. R170605-01132, supervised by the Ministry of SMEs and Startups

Tricell PRP Morocco Product Certification – Certification No. 50624/2023/4381-2024/DM/DPS/DMP/18

Main-Biz Certification (Management-Innovative Small Business) – Certificate No. 230601-03281, supervised by the Ministry of SMEs and Startups

Establishment of Shanghai REV-MED Co., Ltd.

Issuance of Convertible Bonds (Pre-IPO Investment Secured)

Veterinary Medical Device Manufacturing License Acquired

Korea MFDS Approval (Class III): TriCell PRP UNI

Korea MFDS Approval (Class III): Blood Processing Device (NovaStem BC)

Korea MFDS Approval (Class III): Bone Marrow Processing Device (NovaStem BMAC)


Inno-Biz Certification (Technology-Innovative Small Business)

Korea MFDS Approval (Class III): Fat Separation Device (DUOCELL SVF KIT)

ISO 13485: 2018 Certification Acquired

Hilthera 4.0 CE Certification Acquired

2019~2017

  • 2019.01

  • 2018.12

  • 2018.11

  • 2018.09

  • 2018.03

  • 2017.05

  • 2017.03

Taiwan Medical Device Certification: Hilthera 4.0


Development and Commercialization of Bone Marrow Processing Device 


World-Class Product Certification


Development of Large-Capacity 50ml Autologous Bone Marrow Processing Device


Opening of REV-MED Stem Cell Research Institute


Opening of Laser Division


Japan PMDA Approval: Blood Processing Device (Class III, TriCell PRP)  

2016~2009

  • 2016.08 

  • 2016.06 

  • 2016.03 

  • 2015.12

  • 2015.01~2015.12

  • 2014.07~2015.07
     
  • 2013.10

  • 2012.10


  • 2012.07

  • 2009.01

Health Technology (NET) Certification


China CFDA (NMPA) Approval: Blood Processing Device (Class III, TriCell PRP)


Korean MFDS Approval: Bone Marrow Processing Device (Class III, TriCell BMC)


Establishment of REV-MED International GmbH in Germany (Joint Venture)


Blood Processing Device Development (Gyeonggi Science and Technology Promotion Agency)


Development of Autologous Bone Marrow-Derived Stem Cell and Nucleated Cell Concentration Kit 


Opening of Corporate Research Institute

 

ISO 13485: 2012 Certification Acquired

TriCell PRP CE Certification Acquired


Korean MFDS Approval: Blood Processing Device (Class III, TriCell PRP)


Establishment of REV-MED Corporation